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差分脉冲极谱法测定生物流体中的硝基咪唑类化合物。

Determination of nitroimidazoles in biological fluids by differential pulse polarography.

作者信息

Brooks M A, D'Arconte L, de Silva J A

出版信息

J Pharm Sci. 1976 Jan;65(1):112-4. doi: 10.1002/jps.2600650125.

Abstract

A sensitive differential pulse polarographic assay was developed for the determination of metronidazole, ornidazole, and 2-nitro-1H-imidazole-1-(3-methoxy-2-propanol) in plasma. The compounds are selectively extracted into ethyl acetate from a protein-free filtrate of plasma, buffered to pH 7.0 +/- 0.2. The residue of the ethyl acetate extract is dissolved in 0.1 N NaOH and analyzed by differential pulse polarography for the reduction of the nitro group at approximately -0.600 v versus the saturated calomel electrode. The overall recovery from plasma was about 55 +/- 3.0% (SD) for the three compounds investigated. A TLC step after the ethyl acetate extraction may also be included to ensure specificity. This step reduced the overall recovery to approximately 45%. The sensitivity limit of detection from plasma using a 2-ml sample is 0.1 mug/ml. The assay may also be employed for the analysis of urine. The urine is adjusted to pH 7.0 +/- 0.2 and extracted with ethyl acetate, and the residue is analyzed as described for plasma. The assay was applied to the determination of ornidazole in blood and urine in the dog following 10 mg/kg po.

摘要

已开发出一种灵敏的微分脉冲极谱分析法,用于测定血浆中的甲硝唑、奥硝唑和2-硝基-1H-咪唑-1-(3-甲氧基-2-丙醇)。将这些化合物从pH值缓冲至7.0±0.2的血浆无蛋白滤液中选择性萃取到乙酸乙酯中。乙酸乙酯萃取物的残渣溶解于0.1N氢氧化钠中,并通过微分脉冲极谱法分析硝基在相对于饱和甘汞电极约-0.600V处的还原情况。对于所研究的三种化合物,血浆中的总回收率约为55±3.0%(标准差)。乙酸乙酯萃取后也可加入薄层色谱步骤以确保特异性。此步骤使总回收率降至约45%。使用2ml样品时,血浆检测的灵敏度极限为0.1μg/ml。该分析方法也可用于尿液分析。将尿液调节至pH 7.0±0.2,并用乙酸乙酯萃取,残渣按血浆分析方法进行分析。该分析方法用于测定犬口服10mg/kg奥硝唑后血液和尿液中的奥硝唑含量。

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